모든 사진(1)
About This Item
실험식(Hill 표기법):
C13H17NO
CAS Number:
Molecular Weight:
203.28
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22
추천 제품
분석
97%
mp
85-87 °C (lit.)
작용기
ketone
SMILES string
CC(=O)c1ccc(cc1)N2CCCCC2
InChI
1S/C13H17NO/c1-11(15)12-5-7-13(8-6-12)14-9-3-2-4-10-14/h5-8H,2-4,9-10H2,1H3
InChI key
JCMZZYSPSGHBNM-UHFFFAOYSA-N
일반 설명
4′-Piperidinoacetophenone undergoes Claisen-Schmidt condensation with substituted benzaldehydes using NaOH-Al2O3 by microwave irradiation to give chalcones. It has antimycobacterial activity.
애플리케이션
4′-Piperidinoacetophenone was used as internal standard in the determination of pethidine, a narcotic analgesic drug in body fluids by gas chromatography-tandem mass spectrometry.
Pharmacological activity:
- Selective antimycobacterial activity
- Bronchodilator compound
- Modulation of flagellar motility in Chlamydomonas
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
dust mask type N95 (US), Eyeshields, Gloves
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
Microwave enhanced Claisen-Schmidt condensation: A green route to chalcones.
Singh JP, et al.
Indian J. Chem. B, 51(11), 1623-1623 (2012)
Akira Ishii et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 792(1), 117-121 (2003-06-28)
We have presented a simple and sensitive method for determining pethidine, a narcotic analgesic drug in body fluids by gas chromatography-tandem mass spectrometry (GC-MS/MS). Pethidine and 4'-piperidinoacetophenone (internal standard) were extracted from body fluids with Bond Elut C(18) columns; the
L Rajabi et al.
Letters in applied microbiology, 40(3), 212-217 (2005-02-18)
Mycobacteria are a serious cause of infections in humans, with limited treatment options, as no new antibiotics have been developed against mycobacteria since the 1960s. In this study, the antimycobacterial activity of a small library of acetophenone (AP) compounds was
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